JP6344999B2 - 積層体、導電性ローラ及び積層体の製造方法 - Google Patents
積層体、導電性ローラ及び積層体の製造方法 Download PDFInfo
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- JP6344999B2 JP6344999B2 JP2014134841A JP2014134841A JP6344999B2 JP 6344999 B2 JP6344999 B2 JP 6344999B2 JP 2014134841 A JP2014134841 A JP 2014134841A JP 2014134841 A JP2014134841 A JP 2014134841A JP 6344999 B2 JP6344999 B2 JP 6344999B2
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- Prior art keywords
- meth
- acrylate
- base layer
- laminate
- acryloyl group
- Prior art date
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Images
Classifications
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- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/40—Layered products comprising a layer of synthetic resin comprising polyurethanes
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- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D3/00—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials
- B05D3/06—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials by exposure to radiation
- B05D3/061—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials by exposure to radiation using U.V.
- B05D3/065—After-treatment
- B05D3/067—Curing or cross-linking the coating
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D7/00—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials
- B05D7/02—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials to macromolecular substances, e.g. rubber
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- B—PERFORMING OPERATIONS; TRANSPORTING
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US15/321,781 US10442169B2 (en) | 2014-06-30 | 2015-06-26 | Laminated body, conductive roller, and method for manufacturing laminated body |
CN201580033848.7A CN106457802B (zh) | 2014-06-30 | 2015-06-26 | 层叠体、导电性辊和层叠体的制造方法 |
EP15815518.4A EP3162562B1 (de) | 2014-06-30 | 2015-06-26 | Laminat, leitfähiger roller und verfahren zur herstellung von laminat |
PCT/JP2015/003226 WO2016002181A1 (ja) | 2014-06-30 | 2015-06-26 | 積層体、導電性ローラ及び積層体の製造方法 |
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JP6433271B2 (ja) * | 2014-12-03 | 2018-12-05 | キヤノン株式会社 | 電子写真用部材、および電子写真用部材の製造方法 |
US20190041766A1 (en) * | 2016-02-01 | 2019-02-07 | Bridgestone Corporation | Conductive roller, and production method therefor |
JP6924705B2 (ja) | 2016-02-01 | 2021-08-25 | 株式会社ブリヂストン | 帯電ローラ |
JP6778217B2 (ja) * | 2016-02-02 | 2020-10-28 | 株式会社ブリヂストン | 積層体、現像部材及び積層体の製造方法 |
JP6924053B2 (ja) * | 2017-03-17 | 2021-08-25 | 株式会社ブリヂストン | 積層体及び導電性ローラ |
JP6979363B2 (ja) * | 2018-01-30 | 2021-12-15 | 株式会社ブリヂストン | 導電性ローラ及び画像形成装置 |
WO2020009234A1 (ja) * | 2018-07-05 | 2020-01-09 | 株式会社ブリヂストン | 導電性ローラ及び画像形成装置 |
US11460789B2 (en) | 2018-12-17 | 2022-10-04 | Archem Inc. | Charging roller and image forming apparatus |
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US4337296A (en) * | 1980-08-25 | 1982-06-29 | Congoleum Corporation | Methods for bonding dissimilar synthetic polymeric materials and the products involved in and resulting from such methods |
US4634602A (en) * | 1986-01-02 | 1987-01-06 | Ppg Industries, Inc. | Primer composition |
GB9110783D0 (en) * | 1991-05-18 | 1991-07-10 | Ciba Geigy | Adhesives |
JP2000229394A (ja) * | 1999-02-10 | 2000-08-22 | Unitika Ltd | 易接着性ポリエステルフィルム |
DE19964282B4 (de) * | 1999-12-06 | 2004-01-29 | Basf Coatings Ag | Verfahren zur Herstellung einer farb- und/oder effektgebenden Mehrschichtlackierung auf einem grundierten oder ungrundierten Substrat und mit Hilfe des Verfahrens herstellbare Mehrschichtlackierungen |
ATE329976T1 (de) * | 2002-08-22 | 2006-07-15 | Du Pont | Verfahren zum beschichten von faserverstärkten kunststoffsubstraten mit einem primer |
WO2006001171A1 (ja) * | 2004-06-09 | 2006-01-05 | Bridgestone Corporation | 現像ローラ、帯電ローラ、導電性ローラ及びその製造方法 |
US20060173122A1 (en) * | 2005-02-01 | 2006-08-03 | Carmen Flosbach | Non-aqueous, liquid coating compositions curable by free-radical polymerization of olefinic double bonds |
US20070197362A1 (en) * | 2006-02-02 | 2007-08-23 | Bridgestone Corporation | Conductive elastic roller and image forming apparatus comprising the same |
JP4616297B2 (ja) | 2006-03-07 | 2011-01-19 | 株式会社ブリヂストン | 導電性ローラ及びそれを備えた画像形成装置 |
JP4874051B2 (ja) | 2006-10-25 | 2012-02-08 | 株式会社ブリヂストン | 導電性ローラ及びそれを備えた画像形成装置 |
JP4657263B2 (ja) * | 2007-07-17 | 2011-03-23 | 株式会社ブリヂストン | 現像ローラ |
US7740265B2 (en) * | 2008-07-02 | 2010-06-22 | Lundin Recovery Equipment Llc | Semi tractor dolly assembly |
WO2012105615A1 (ja) | 2011-02-01 | 2012-08-09 | 株式会社ブリヂストン | 現像ローラ |
CN102673211B (zh) | 2011-03-09 | 2016-01-20 | Dic株式会社 | 活性能量射线固化性转印片材及其制造方法 |
JP5815994B2 (ja) * | 2011-06-03 | 2015-11-17 | 株式会社ブリヂストン | 現像ローラ |
JP6034779B2 (ja) * | 2012-12-28 | 2016-11-30 | 大日精化工業株式会社 | 高耐久機能性成型シート及びそれを用いて得られる加飾成型品 |
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JP2016010949A (ja) | 2016-01-21 |
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